Variant report

Variant	nsv869186
Chromosome Location	chrX:78392001-79166725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2481)
CpG islands
(count:610)
Chromatin interactive
region (count:33)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2481 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:78705834-78706050	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:78619848-78620082	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:78705812-78706026	K562	blood:	n/a	n/a
4	ATF2	chrX:78514299-78515411	GM12878	blood:	n/a	n/a
5	ATF2	chrX:78417110-78417676	GM12878	blood:	n/a	n/a
6	ATF2	chrX:78518986-78519407	GM12878	blood:	n/a	n/a
7	ATF2	chrX:78417058-78417611	GM12878	blood:	n/a	n/a
8	ATF2	chrX:78399710-78400337	GM12878	blood:	n/a	n/a
9	ATF2	chrX:78394218-78394817	GM12878	blood:	n/a	n/a
10	ATF2	chrX:78437903-78438672	GM12878	blood:	n/a	n/a
11	ATF2	chrX:78421281-78421725	GM12878	blood:	n/a	n/a
12	ATF2	chrX:78525814-78526271	GM12878	blood:	n/a	n/a
13	ATF2	chrX:78437932-78438662	GM12878	blood:	n/a	n/a
14	ATF2	chrX:78525744-78526290	GM12878	blood:	n/a	n/a
15	ATF2	chrX:78514368-78515342	GM12878	blood:	n/a	n/a
16	ATF3	chrX:78409960-78410104	GM12878	blood:	n/a	n/a
17	BACH1	chrX:78622927-78623123	K562	blood:	n/a	n/a
18	BACH1	chrX:79147511-79147702	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chrX:78417201-78417512	GM12878	blood:	n/a	chrX:78417268-78417277 chrX:78417296-78417305
20	BATF	chrX:78885743-78886112	GM12878	blood:	n/a	n/a
21	BATF	chrX:78438083-78438617	GM12878	blood:	n/a	n/a
22	BATF	chrX:78438108-78438518	GM12878	blood:	n/a	n/a
23	BATF	chrX:78735482-78735650	GM12878	blood:	n/a	n/a
24	BATF	chrX:78417220-78417532	GM12878	blood:	n/a	chrX:78417268-78417277 chrX:78417296-78417305
25	BATF	chrX:78415317-78415638	GM12878	blood:	n/a	n/a
26	BATF	chrX:78525986-78526219	GM12878	blood:	n/a	n/a
27	BATF	chrX:78885772-78886094	GM12878	blood:	n/a	n/a
28	BATF	chrX:78403024-78403295	GM12878	blood:	n/a	n/a
29	BATF	chrX:78514439-78515213	GM12878	blood:	n/a	n/a
30	BATF	chrX:78514438-78514939	GM12878	blood:	n/a	n/a
31	BATF	chrX:78514941-78515217	GM12878	blood:	n/a	n/a
32	BCL11A	chrX:78417173-78417550	GM12878	blood:	n/a	n/a
33	BCL11A	chrX:78394379-78394649	GM12878	blood:	n/a	n/a
34	BCL11A	chrX:78438020-78438486	GM12878	blood:	n/a	chrX:78438333-78438342
35	BCL11A	chrX:78514467-78515304	GM12878	blood:	n/a	n/a
36	BCL11A	chrX:78514521-78515215	GM12878	blood:	n/a	n/a
37	BCL11A	chrX:78438085-78438604	GM12878	blood:	n/a	chrX:78438333-78438342
38	BCL3	chrX:78421335-78421663	GM12878	blood:	n/a	n/a
39	BCL3	chrX:78417175-78417506	GM12878	blood:	n/a	n/a
40	BCL3	chrX:78437980-78438576	GM12878	blood:	n/a	chrX:78438333-78438342
41	BCL3	chrX:78514571-78515206	GM12878	blood:	n/a	n/a
42	BCL3	chrX:78514410-78515255	GM12878	blood:	n/a	n/a
43	BCL3	chrX:78438138-78438532	GM12878	blood:	n/a	chrX:78438333-78438342
44	BCLAF1	chrX:78525901-78526305	GM12878	blood:	n/a	n/a
45	BCLAF1	chrX:78394195-78394795	GM12878	blood:	n/a	n/a
46	BCLAF1	chrX:78514376-78515369	GM12878	blood:	n/a	n/a
47	BCLAF1	chrX:78437991-78438567	GM12878	blood:	n/a	chrX:78438333-78438342
48	BCLAF1	chrX:78394322-78394739	GM12878	blood:	n/a	n/a
49	BCLAF1	chrX:78437977-78438673	GM12878	blood:	n/a	chrX:78438333-78438342
50	BCLAF1	chrX:78399746-78400258	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:78623020-78623070	GM12878	blood:	n/a
2	chrX:78622565-78622615	GM12891	blood:	n/a
3	chrX:78623745-78623795	NHDF-neo	bronchial:	n/a
4	chrX:78623020-78623070	HEEpiC	esophagus:	n/a
5	chrX:78426877-78426927	HRCEpiC	kidney:	n/a
6	chrX:78400174-78400224	IMR90	lung:	fetal
7	chrX:78400174-78400224	NHBE	bronchial:	n/a
8	chrX:78623020-78623070	HCT-116	colon:	n/a
9	chrX:78400174-78400224	MCF10A-Er-Src	breast:	n/a
10	chrX:78623745-78623795	Hepatocyte	liver:	n/a
11	chrX:78623956-78624006	GM19239	blood:	n/a
12	chrX:78624108-78624158	GM12878	blood:	n/a
13	chrX:78426877-78426927	AG09319	gingival:	n/a
14	chrX:78624108-78624158	HEEpiC	esophagus:	n/a
15	chrX:78623745-78623795	GM06990	blood:	n/a
16	chrX:78623020-78623070	MCF-7	breast:	n/a
17	chrX:78624108-78624158	SAEC	small airway:	n/a
18	chrX:78623020-78623070	Hepatocyte	liver:	n/a
19	chrX:78622682-78622732	Hepatocyte	liver:	n/a
20	chrX:78623745-78623795	H1-hESC	embryonic stem cell:	embryo
21	chrX:78427682-78427732	Hela-S3	cervix:	n/a
22	chrX:78400174-78400224	SK-N-SH	brain:	n/a
23	chrX:78426877-78426927	PANC-1	pancreas:	n/a
24	chrX:78623956-78624006	HEEpiC	esophagus:	n/a
25	chrX:78624108-78624158	Caco-2	colon:	n/a
26	chrX:78622565-78622615	HRPEpiC	eye:	n/a
27	chrX:78622859-78622909	CMK	blood:	n/a
28	chrX:78622682-78622732	NHBE	bronchial:	n/a
29	chrX:78622682-78622732	AG04449	skin:	fetal
30	chrX:78400174-78400224	H1-hESC	embryonic stem cell:	embryo
31	chrX:78427682-78427732	LNCaP	prostate:	n/a
32	chrX:78427682-78427732	T-47D	breast:	n/a
33	chrX:78426877-78426927	HEEpiC	esophagus:	n/a
34	chrX:78622682-78622732	NB4	blood:	n/a
35	chrX:78427682-78427732	SAEC	small airway:	n/a
36	chrX:78427682-78427732	BJ	skin:	n/a
37	chrX:78426877-78426927	HUVEC	blood vessel:	n/a
38	chrX:78623956-78624006	ovcar-3	ovarian:	n/a
39	chrX:78622565-78622615	GM12892	blood:	n/a
40	chrX:78623745-78623795	HCM	heart:	n/a
41	chrX:78400174-78400224	HCM	heart:	n/a
42	chrX:78624108-78624158	Hepatocyte	liver:	n/a
43	chrX:78623745-78623795	AG04449	skin:	fetal
44	chrX:78622859-78622909	HCF	heart:	n/a
45	chrX:78624108-78624158	GM12891	blood:	n/a
46	chrX:78622565-78622615	NT2-D1	testis:	n/a
47	chrX:78622859-78622909	HCM	heart:	n/a
48	chrX:78623956-78624006	SAEC	small airway:	n/a
49	chrX:78623956-78624006	H1-hESC	embryonic stem cell:	embryo
50	chrX:78426877-78426927	K562	blood:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:79111031..79113848-chrX:79129901..79131563,2	K562	blood:
2	chrX:78623909..78625908-chrX:78627039..78629119,3	K562	blood:
3	chr2:219180197..219181031-chrX:78672273..78672996,2	HCT-116	colon:
4	chrX:79105661..79108257-chrX:79112036..79113785,2	MCF-7	breast:
5	chr17:56706703..56709057-chrX:78429769..78431270,3	MCF-7	breast:
6	chrX:78884290..78886421-chrX:78889264..78891291,2	K562	blood:
7	chr2:68478772..68479685-chrX:79123890..79124390,2	Hela-S3	cervix:
8	chrX:79132290..79134398-chrX:79136094..79138656,2	MCF-7	breast:
9	chr8:110352840..110355386-chrX:78849788..78852363,2	MCF-7	breast:
10	chrX:79111031..79113848-chrX:79129901..79131563,2	K562	blood:
11	chrX:78611688..78613722-chrX:78621637..78623492,2	K562	blood:
12	chr11:118881446..118882428-chrX:78719744..78720315,2	MCF-7	breast:
13	chrX:77810661..77811278-chrX:78780189..78780762,2	MCF-7	breast:
14	chr9:119319099..119319741-chrX:79019251..79019874,2	MCF-7	breast:
15	chrX:78600900..78603777-chrX:78604763..78607370,2	MCF-7	breast:
16	chrX:78884290..78886421-chrX:78889264..78891291,2	K562	blood:
17	chrX:78615570..78618200-chrX:78620529..78622334,2	K562	blood:
18	chr8:55770247..55770767-chrX:78893853..78894478,2	MCF-7	breast:
19	chrX:79132290..79134398-chrX:79136094..79138656,2	MCF-7	breast:
20	chrX:78615570..78618200-chrX:78620529..78622334,2	K562	blood:
21	chrX:78828818..78830377-chrX:78830400..78832363,2	MCF-7	breast:
22	chrX:78600900..78603777-chrX:78604763..78607370,2	MCF-7	breast:
23	chr15:79105202..79107134-chrX:78755858..78757584,2	MCF-7	breast:
24	chrX:78525004..78527679-chrX:78527827..78529683,2	MCF-7	breast:
25	chrX:77811500..77813088-chrX:78666250..78667785,2	MCF-7	breast:
26	chrX:78828818..78830377-chrX:78830400..78832363,2	MCF-7	breast:
27	chrX:78613371..78615323-chrX:78622479..78624740,2	K562	blood:
28	chrX:78525004..78527679-chrX:78527827..78529683,2	MCF-7	breast:
29	chrX:79105661..79108257-chrX:79112036..79113785,2	MCF-7	breast:
30	chrX:78612180..78614323-chrX:78618566..78621520,2	K562	blood:
31	chr17:56706259..56709497-chrX:78429768..78431270,3	MCF-7	breast:
32	chrX:78733188..78733978-chrX:79285640..79286468,2	MCF-7	breast:
33	chrX:78615804..78618128-chrX:78622582..78624536,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR174-1	chrX:78412319-78412416	NONHSAT137711
2	lnc-ITM2A-3	chrX:78432697-78433165	NONHSAT137712
3	lnc-ITM2A-2	chrX:78624861-78625662	NONHSAT137716
4	lnc-GPR174-1	chrX:78400551-78400714	NONHSAT137711

No data

Variant related genes	Relation type
GPR174	TF binding region
KIF4CP	TF binding region
ENSG00000271005	TF binding region
ENSG00000270268	TF binding region
ITM2A	TF binding region
GPR174	CpG island
KIF4CP	CpG island
ENSG00000271005	CpG island
ENSG00000270268	CpG island
ITM2A	CpG island
ENSG00000078596	chromatin interactions
ENSG00000270268	chromatin interactions
ENSG00000186166	chromatin interactions
ENSG00000221823	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 4375 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:4375 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12688044	chrX:78392028-78392029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189232637	chrX:78392165-78392166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374262429	chrX:78392272-78392273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200351936	chrX:78392345-78392346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372245702	chrX:78392346-78392347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376062877	chrX:78392347-78392348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201148668	chrX:78392363-78392364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565322824	chrX:78392435-78392436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181986504	chrX:78392585-78392586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532667589	chrX:78392593-78392594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147446698	chrX:78392595-78392596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186313198	chrX:78392599-78392600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1832279	chrX:78392654-78392655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189595429	chrX:78392888-78392889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371386400	chrX:78392935-78392936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145499533	chrX:78393029-78393030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112933952	chrX:78393128-78393129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs5912769	chrX:78393144-78393145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201459386	chrX:78393151-78393152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199690715	chrX:78393152-78393153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35908025	chrX:78393153-78393154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376600092	chrX:78393154-78393155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs66696453	chrX:78393163-78393164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397896841	chrX:78393174-78393175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370757612	chrX:78393303-78393304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375517825	chrX:78393327-78393328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182620824	chrX:78393341-78393342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186511695	chrX:78393497-78393498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191377591	chrX:78393529-78393530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183586143	chrX:78393580-78393581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs36012508	chrX:78394014-78394015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187635815	chrX:78394070-78394071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201020529	chrX:78394259-78394260	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs192228406	chrX:78394357-78394358	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs540792623	chrX:78394473-78394474	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs183283953	chrX:78394542-78394543	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs187904689	chrX:78394627-78394628	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs147688177	chrX:78394662-78394663	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs200763400	chrX:78394667-78394668	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs559426226	chrX:78394813-78394814	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148668129	chrX:78394838-78394839	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191262927	chrX:78394879-78394880	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2411975	chrX:78395070-78395071	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs548134333	chrX:78395085-78395086	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201217982	chrX:78395097-78395098	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538505754	chrX:78395137-78395138	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6652306	chrX:78395181-78395182	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111264127	chrX:78395242-78395243	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533803561	chrX:78395272-78395273	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577761414	chrX:78395277-78395278	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Autism	22495311	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Premature ovarian failure	20952765	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:78389600-78394600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chrX:78390200-78394400	Weak transcription	Primary T cells from cord blood	blood
3	chrX:78390400-78394000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chrX:78390600-78393400	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chrX:78390600-78393800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chrX:78390800-78393600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chrX:78391000-78393600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chrX:78391000-78394000	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chrX:78391000-78394000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chrX:78391200-78394000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chrX:78391200-78394400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chrX:78391400-78393400	Weak transcription	Primary B cells from peripheral blood	blood
13	chrX:78393200-78394200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chrX:78393200-78394200	Enhancers	Dnd41	blood
15	chrX:78393400-78395200	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chrX:78393400-78396200	Enhancers	Primary B cells from peripheral blood	blood
17	chrX:78393600-78394400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chrX:78393600-78394400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chrX:78393600-78396400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chrX:78393600-78396600	Enhancers	Primary B cells from cord blood	blood
21	chrX:78393600-78396600	Enhancers	Primary hematopoietic stem cells	blood
22	chrX:78393600-78400400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chrX:78393800-78394000	Flanking Active TSS	GM12878-XiMat	blood
24	chrX:78393800-78395200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chrX:78393800-78395400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chrX:78393800-78396200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chrX:78394000-78394200	Enhancers	GM12878-XiMat	blood
28	chrX:78394000-78395400	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chrX:78394000-78395400	Enhancers	Monocytes-CD14+_RO01746	blood
30	chrX:78394000-78395600	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chrX:78394000-78396000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chrX:78394000-78396400	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chrX:78394200-78394400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chrX:78394200-78394400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chrX:78394200-78394800	Flanking Active TSS	Dnd41	blood
36	chrX:78394200-78395000	Flanking Active TSS	GM12878-XiMat	blood
37	chrX:78394400-78394600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chrX:78394400-78394800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
39	chrX:78394400-78394800	Enhancers	Fetal Thymus	thymus
40	chrX:78394400-78395200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chrX:78394400-78395400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chrX:78394400-78395400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chrX:78394400-78395400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chrX:78394400-78395600	Enhancers	Primary T cells from cord blood	blood
45	chrX:78394600-78395400	Enhancers	Primary T cells fromperipheralblood	blood
46	chrX:78394600-78395400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chrX:78394800-78396200	Enhancers	Dnd41	blood
48	chrX:78394800-78396400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chrX:78394800-78399400	Weak transcription	Fetal Thymus	thymus
50	chrX:78395000-78396000	Enhancers	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links